Antimicrobial Dihydroflavonols and Isoflavans Isolated from the Root Bark of <i>Dalbergia gloveri</i>

Three new dihydroflavonols, gloverinols A-C (<b>1</b>-<b>3</b>), a new flavon-3-ol, gloverinol D (<b>4</b>), two new isoflavans, gloveriflavan A (<b>5</b>) and B (<b>6</b>), and seven known compounds were isolated from the root bark of <i>Dalbergia gloveri</i>. The structures of the isolates were elucidated by using NMR, ECD, and HRESIMS data analyses. Among the isolated compounds, gloverinol B (<b>2</b>), gloveriflavan B (<b>6</b>), and 1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphenyl)-1-propanone (<b>10</b>) were the most active against <i>Staphylococcus aureus</i>, with MIC values of 9.2, 18.4, and 14.2 μM, respectively.

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Publication Details

Journal
Journal of Natural Products
Published
2024-09-10
DOI
https://doi.org/10.1021/acs.jnatprod.4c00690
Citations
8
Primary Topic
Bioactive natural compounds
Type
article
Field-Weighted Citation Impact
1.87

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article

Antimicrobial Dihydroflavonols and Isoflavans Isolated from the Root Bark of Dalbergia gloveri

Duncan Mutiso Chalo, Vaderament‐A. Nchiozem‐Ngnitedem, Albert Ndakala, Daniel Umereweneza et al.
8 citations
Journal of Natural Products
Bioactive natural compounds
1.87
article

Antimicrobial Dihydroflavonols and Isoflavans Isolated from the Root Bark of Dalbergia gloveri

Duncan Mutiso Chalo, Vaderament‐A. Nchiozem‐Ngnitedem, Albert Ndakala, Daniel Umereweneza, Máté Erdélyi, Ruisheng Xiong, Ivan Kiganda, Wouter Herrebout, Abiy Yenesew, Lianne H. E. Wieske, Tomasz M. Karpiński
article en
8 citations

Abstract

Three new dihydroflavonols, gloverinols A-C (<b>1</b>-<b>3</b>), a new flavon-3-ol, gloverinol D (<b>4</b>), two new isoflavans, gloveriflavan A (<b>5</b>) and B (<b>6</b>), and seven known compounds were isolated from the root bark of <i>Dalbergia gloveri</i>. The structures of the isolates were elucidated by using NMR, ECD, and HRESIMS data analyses. Among the isolated compounds, gloverinol B (<b>2</b>), gloveriflavan B (<b>6</b>), and 1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphenyl)-1-propanone (<b>10</b>) were the most active against <i>Staphylococcus aureus</i>, with MIC values of 9.2, 18.4, and 14.2 μM, respectively.

Journal of Natural ProductsVol. 87(9)
Poznan University of Medical Sciences (PL), Uppsala University (SE), University of Nairobi (KE), University of Antwerp (BE), University of Rwanda (RW)
Vetenskapsrådet
Life in Land
Openalex Percentile: Top 14%
Bioactive natural compounds
1.87
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